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Central nervous system involvement in arthrogryposis multiplex congenita: Overview of causes, diagnosis, and care

Artikel i vetenskaplig tidskrift
Författare K. Dieterich
Eva Kimber
J. G. Hall
Publicerad i American Journal of Medical Genetics Part C-Seminars in Medical Genetics
ISSN 1552-4868
Publiceringsår 2019
Publicerad vid Institutionen för kliniska vetenskaper, Avdelningen för pediatrik
Språk en
Länkar dx.doi.org/10.1002/ajmg.c.31732
Ämnesord arthrogryposis multiplex congenita, neonatally lethal AMC syndromes, central nervous system, prader-willi-syndrome, spinal muscular-atrophy, mutations, contractures, etiology, form, classification, hypoplasia, genetics, f3/contactin, Genetics & Heredity, netics
Ämneskategorier Klinisk medicin


Arthrogryposis or AMC, arthrogryposis multiplex congenita, is defined as multiple congenital joint contractures in more than two joints and in different body areas. The common cause of all AMC is lack of movement in utero, which in turn can have different causes, one of which is CNS involvement. Intellectual disability/CNS involvement is found in approximately 25% of all AMC. AMC with CNS involvement includes a large number of genetic syndromes. So far, more than 400 genes have been identified as linked to AMC, with and without CNS involvement. A number of neonatally lethal syndromes and syndromes resulting in severe disability due to CNS malfunction belong to this group of syndromes. There are several X-linked disorders with AMC, which are primarily related to intellectual disability. A number of neuromuscular disorders may include AMC and CNS/brain involvement. Careful clinical evaluation by a geneticist and a pediatrician/pediatric neurologist is the first step in making a specific diagnosis. Further investigations may include MRI of the brain and spinal cord, electroencephalogram, blood chemistry for muscle enzymes, other organ investigations (ophtalmology, cardiology, gastrointestinal, and genitourinary systems). Nerve conduction studies, electromyogram, and muscle pathology may be of help when there is associated peripheral nervous system involvement. But most importantly, genetic investigations with targeted or rather whole exome or genome sequencing should be performed. A correct diagnosis is important in planning adequate treatment, in genetic counselling and also for future understanding of pathogenic mechanisms and possible new treatments. A multidiciplinary team is needed both in investigation and treatment.

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